FDA 510(k), K063503, OPTIVANTAGE DH INJECTOR SYSTEM WITH ENHANCED COMMUNICATION

FDA 510(k), K063503, OPTIVANTAGE DH INJECTOR SYSTEM WITH ENHANCED COMMUNICATION

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510(K) Number: K063503
Device Name: OPTIVANTAGE DH INJECTOR SYSTEM WITH ENHANCED COMMUNICATION
Manufacturer:
Device Classification Name: Injector, Contrast Medium, Automatic
Regulation Number: 870.1650
Classification Product Code: IZQ
Date Received: 11/20/2006
Decision Date: 04/27/2007
Regulation Medical Specialty: Cardiovascular
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